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D.B. Westjohn

Publications and source records attributed to D.B. Westjohn.

6 recordsLinked to original sources

Arsenic in ground water of the United States: occurrence and geochemistry

Concentrations of naturally occurring arsenic in ground water vary regionally due to a combination of climate and geology. Although slightly less than half of 30,000 arsenic analyses of ground water in the United States were 1 μg/L, about 10% exceeded 10 μg/L. At a broad regional scale, arsenic concentrations exceeding 10 μg/L appear to be more frequently observed in the western United States than in the eastern half. Arsenic concentrations in ground water of the Appalachian Highlands and the Atlantic Plain generally are very low ( 1 μg/L). Concentrations are somewhat greater in the Interior Plains and the Rocky Mountain System. Investigations of ground water in New England, Michigan, Minnesota, South Dakota, Oklahoma, and Wisconsin within the last decade suggest that arsenic concentrations exceeding 10 μg/L are more widespread and common than previously recognized. Arsenic release from iron oxide appears to be the most common cause of widespread arsenic concentrations exceeding 10 μg/L in ground water. This can occur in response to different geochemical conditions, including release of arsenic to ground water through reaction of iron oxide with either natural or anthropogenic (i.e., petroleum products) organic carbon. Iron oxide also can release arsenic to alkaline ground water, such as that found in some felsic volcanic rocks and alkaline aquifers of the western United States. Sulfide minerals are both a source and sink for arsenic. Geothermal water and high evaporation rates also are associated with arsenic concentrations 10g/L in ground and surface water, particularly in the west. Arsenic release from iron oxide appears to be the most common cause of widespread arsenic concentrations exceeding 10 µg/L a ground water. This can occur in response to different geochemical conditions, including release of arsenic to ground water through reaction of iron oxide with either natural or anthropogenic (i.e., petroleum products) organic carbon. Iron oxide also can release arsenic to alkaline ground water, such as that found in some felsic volcanic rocks and alkaline aquifers of the Western United States. Sulfide minerals are both a source and sink for arsenic. Geothermal water and high evaporation rates also are associated with arsenic concentrations ≥ 10g/L in ground and surface water, particularly in the west.

Ground Water

Simulation of ground-water flow and areas contributing ground water to production wells, Cadillac, Michigan

Ground water is the primary source of water for domestic, municipal, and industrial use within the northwest section of Michigan's Lower Peninsula. Because of the importance of this resource, numerous communities including the city of Cadillac in Wexford County, Michigan, have begun local well-head protection programs. In these programs, communities protect their ground-water resources by identifying the areas that contribute water to production wells, identifying potential sources of contamination, and developing methods to cooperatively manage and minimize threats to the water supply. The U.S. Geological Survey, in cooperation with the city of Cadillac, simulated regional ground-water flow and estimated areas contributing recharge and zones of transport to the production well field. Ground-water flow models for the Clam River watershed, in Wexford and Missaukee Counties, were developed using the U.S. Geological Survey modular three-dimensional finite-difference ground-water flow model (MODFLOW 2000). Ground-water flow models were calibrated using the observation, sensitivity, and parameter estimation packages of MODFLOW 2000. Ground-water-head solutions from calibrated flow models were used in conjunction with MODPATH, a particle-tracking program, to simulate regional ground-water flow and estimate areas contributing recharge and zones of transport to the Cadillac production-well field for a 10-year period. Model simulations match the conceptual model in that regional ground-water flow in the deep ground-water system is from southeast to northwest across the watershed. Areas contributing water were determined for the optimized parameter set and an alternate parameter set that included increased recharge and hydraulic conductivity values. Although substantially different hydrologic parameters (assumed to represent end-member ranges of realistic hydrologic parameters) were used in alternate numerical simulations, simulation results differ little in predictions of the size of the contributing area to the city well field. However, increasing recharge and hydraulic conductivity values appreciably affected the shape of the contributing area and zone of contribution of reacharge. Simulation results indicate that the region immediately to the south and southeast of the well field is contributing water to the production wells. Detailed aquifer characterization would be needed to describe and simulate

Michigan

Arsenic in southeastern Michigan

Arsenic levels exceeding 10 μg/L are present in hundreds of private supply wells distributed over ten counties in eastern and southeastern Michigan. Most of these wells are completed in the Mississippian Marshall Sandstone, the principal bedrock aquifer in the region, or in Pleistocene glacial or Pennsylvanian bedrock aquifers. About 70% of ground water samples taken from more than 100 wells, have arsenic contents ≥10 μg/L with a maximum value of 220 μg/L . Water samples and continuous cores were taken from two test wells. Arsenic content of core samples ranges from <5 to more than 300 ppm, with the highest values found for pyritic black shales. Authigenic cements in the Marshall Sandstone include patchy authigenic pyrite that locally contains arsenic-rich (up to 8.5 wt. % As) domains. Bulk arsenic contents of pyrite-bearing intervals, sampled in well cuttings, are a high as 1020 ppm. Arsenic-rich pyrite is likely the ultimate source of arsenic in eastern and southeastern Michigan ground water, but evidence for pyrite oxidation at depth in bedrock aquifers is generally lacking. Pyrite oxidation may occur or have occurred in tills derived from the Marshall Sandstone and Coldwater Shale, which were found to contain arsenic-rich (up to at least 0.7 wt. % As) iron oxyhydroxides. Plausible mechanisms for widespread arsenic mobilization in eastern and southeastern Michigan ground water include weathering of pyrite in tills, reductive dissolution of iron oxyhydroxides in tills, and potentially, pyrite oxidation in bedrock aquifers, due to drawdown in wells or lowering of water-table levels in response to Pleistocene glaciation.

Michigan

Methanogenic biodegradation of charcoal production wastes in groundwater at Kingsford, Michigan, USA

A house exploded in the City of Kingsford, Michigan USA. The explosion was caused by CH4 that leaked into the basement from the surrounding soil. Evidence suggests that biodegradation of products from the distillation and spillage at or near a former wood carbonization plant site was the major source of CH4 and CO2 in the groundwater system. The plant area is directly upgradient from deep groundwater, samples of which are green-yellow in colour, have a very strong odour of burnt wood, contain high concentrations of mononuclear aromatic and phenolic compounds, and extremely high concentrations of volatile fatty acids. The majority of the dissolved compounds in these groundwater samples have been shown, using laboratory microcosms, to be anaerobically biodegradable to CH4 and CO2. The biodegradable compounds, and the amounts of CH4 and CO2 produced in the microcosms, are consistent with observations from field samples.

Michigan

Direct-current vertical electrical-resistivity soundings in the Lower Peninsula of Michigan

Ninety-three direct-current vertical electrical-resistivity soundings were conducted in the Lower Peninsula of Michigan from June through October 1987. These soundings were made to assist in mapping the depth to brine in areas where borehole resistivity logs and water-quality data are sparse or lacking. The Schlumberger array for placement of current and potential electrodes was used for each sounding. Vertical electrical-resistivity sounding field data, shifted and smoothed sounding data, and electric layers calculated using inverse modeling techniques are presented. Also included is a summary of the near-surface conditions and depths to conductors and resistors for each sounding location.

Michigan